HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 278248Generated: October 26, 2026
Triethylamine → 4-Piperidinemethanol, 1-benzoyl-
https://huagongshe.com/reaction/278248
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Isobutyl chloroformate | HCID 62365 | — |
| Reactant | 1-Benzoylpiperidine-4-carboxylic acid | HCID 78935 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Piperidinemethanol, 1-benzoyl- | HCID 10262870 | 99.2% |
Reaction Steps
To a solution of 2 g of 1-benzoylisonipecotic acid (Step A) in 50 mL THF at 0° C. were added 1.47 g of triethylamine and 1.99 g of isobutyl chloroformate. The reaction was stirred for 1 h at 0° C. To a solution of 1.10 g of sodium borohydride in 30 mL DMF at 0° C. was slowly added the above THF mixture. The reaction was again stirred for 1 h at 0° C. Water (80 mL) was slowly added to the reaction and the mixture was extracted 5×80 mL ethyl acetate and the combined organic layers were dried over magnesium sulfate. The solvent was then evaporated under reduced pressure. The residue was purified by flash chromatography with 1:1 hexane : ethyl acetate followed by hexane : ethyl acetate: methanol, 50:50:5 to give 1.865 g of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06358979B1 |
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| Source dataset | uspto-grants-2002_03 |
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| ORD ID | ord-ac9768a399e142d29cfd64358aaa3407 |
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| Source note | uspto-grants-2002_03 |
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